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Comparison between Femoral Nerve Anesthesia and Adductor Canal Anesthesia in analgesia and mobility in patients undergoing Revision knee prosthesis surgery randomized controlled clinical trial

Comparison between Femoral Nerve Block and Adductor Canal Block in analgesia and mobility in patients undergoing Revision total knee Arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2n5b5y3
Enrollment
Unknown
Registered
2024-08-08
Start date
2021-09-25
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroplasty

Interventions

This is a two-arm, double-blind, randomized controlled clinical study. A total of 32 participants who meet the eligibility criteria will be probabilistically allocated to one or another intervention g
A08.800.800.720.450.250

Sponsors

Ministério da Saúde
Lead Sponsor
Instituto Nacional de Traumatologia e Ortopedia
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing total knee arthroplasty revision surgery; both sexes; older than 18 years; classified by the American Society of Anesthesiology (ASA) as physical status I to III

Exclusion criteria

Exclusion criteria: Patients with daily consumption of opioids and/or antidepressants; patients in whom it was necessary to perform general anesthesia; patients with neurological and muscular diseases; patients allergic to dipyrone, tramadol and local anesthetics; bedridden and amputated patients; and patients with grade III obesity (BMI > 40)

Design outcomes

Primary

MeasureTime frame
Assess the intensity of pain, at rest and movement, 24 and 48 hours after surgery—

Secondary

MeasureTime frame
Quantify opioid consumption 24 and 48 hours postoperatively;Assess the lifting capacity of the operated limb 24 and 48 hours after surgery;Assess the patient's ability to remain in an orthostatic position 24 and 48 hours postoperatively;Assess the ability to walk 24 and 48 hours postoperatively—

Countries

Brazil

Contacts

Public ContactVitor Santos

Instituto Nacional de Traumatologia e Ortopedia

vitorsbsantos@gmail.com+55-21-21345000

Outcome results

None listed

Source: REBEC (via WHO ICTRP)